No Evidence for an Effect of COMT Val158Met Genotype on Executive Function in Patients With 22q11 Deletion Syndrome von Glaser, Bronwyn, Debbane, Martin, Hinard, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Eliez, Stephan

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Language skills in children with velocardiofacial syndrome (deletion 22q11.2) von Glaser, Bronwyn, Mumme, Donna L., Blasey, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Reiss, Allan L., Eliez, Stephan

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Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility von Paoloni-Giacobino, A, Kern1, I, Rumpler, Y, Djlelati, R, Morris, MA, Dahoun, SP

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Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level von BARBER, J. C. K, REED, C. J, DAHOUN, S. P, JOYCE, C. A

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Fetus with a 9q22q34 interstitial deletion and hygroma von Paoloni-Giacobino, A., Floris, E., Dahoun, S. P.

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Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome von Paoloni-Giacobino, A, Morris, M A, Dahoun, S P

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A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysis von Paoloni-Giacobino, A, Dutoit, Mh, Morris, Ma, Dahoun, Sp

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A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography von Paoloni-Giacobino, A., Dahoun, S. P., Sizonenko, P. C., Stalberg, A., Chardonnens, D., Campana, A.

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Parental Origin of the Deletion 22q11.2 and Brain Development in Velocardiofacial Syndrome: A Preliminary Study von Eliez, Stephan, Antonarakis, Stylianos E, Morris, Michael A, Dahoun, Sophie P, Reiss, Allan L

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A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH von Paoloni-Giacobino, A, Lespinasse, J, Moix, I, Dahoun, S.P

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